BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LADAR WAVE CUSTOM CORNEA WAVEFRONT SYSTEM

    MDR report key: 1040346 · Received May 7, 2008

    Report

    Report Number
    MW5006788
    Event Type
    Injury
    Date Received
    May 7, 2008
    Date of Event
    June 4, 2004
    Report Date
    May 7, 2008
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    POST LASIK EYE SURGERY CHRONIC PROBLEMS AND DISABILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LADAR WAVE CUSTOM CORNEA WAVEFRONT SYSTEM LASIK LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Required Intervention DOXYCYCLENE| DROPS| PLUGS| OMEGA-3 SUPPLEMENTS| READERS| CONTACTS| LID SCRUB| HOT COMPRESS| RX AND OVER-THE-COUNTER: RESTASIS| SUNGLASSES